Medical Device Manufacturer · US , Lake Zurich , IL

Fenwal, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2008

Total

Cleared

Denied

Fenwal, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lake Zurich, US.

Historical record: 3 cleared submissions from 2008 to 2014. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Fenwal, Inc. Filter by specialty or product code using the sidebar.

Fenwal, Inc. is one of 26107 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Fenwal, Inc.

3 devices

1-3 of 3